Reviewed on 12/28/2021

What Is Aducanumab and How Does It Work?

Aducanumab is a prescription medication used to treat Alzheimer's Disease. 

  • Aducanumab is available under the following different brand names: Aduhelm, aducanumab-avwa 

What Are Dosages of Aducanumab?

Adult dosage

Injectable solution

  • 100mg/mL (1.7-mL, 3-mL single-dose vials) 
  • Alzheimer Disease
  • Adult dosage
  • Administered as an IV infusion every 4 weeks and at least 21 days apart
  • Infusions 1-2: 1mg/kg IV every 4 weeks
  • Infusions 3-4: 3mg/kg IV every 4 weeks
  • Infusions 5-6: 6mg/kg IV every 4 weeks
  • Infusion 7 and beyond: 10 mg/kg IV every 4 weeks

Dosage Considerations – Should be Given as Follows

  • See “Dosages”

What Are Side Effects Associated with Using Aducanumab?

Common side effects of Aducanumab include:

  • changes in mental state, 
  • confusion, 
  • vomiting, 
  • nausea, 
  • tremor
  • gait disturbances, 
  • headache, and 
  • falls

Serious side effects of Aducanumab include:

  • hives, 
  • difficulty breathing, 
  • swelling of the face, lips, tongue, or throat, 
  • headaches, 
  • dizziness, 
  • confusion, 
  • nausea, and
  • vision changes

Rare side effects of Aducanumab include:

  • none 

This is not a complete list of side effects and other serious side effects or health problems may occur as a result of the use of this drug. Call your doctor for medical advice about serious side effects or adverse reactions. You may report side effects or health problems to FDA at 1-800-FDA-1088.


Dementia, Alzheimer's Disease, and Aging Brains See Slideshow

What Other Drugs Interact with Aducanumab?

If your medical doctor is using this medicine to treat your pain, your doctor or pharmacist may already be aware of any possible drug interactions and may be monitoring you for them. Do not start, stop, or change the dosage of any medicine before checking with your doctor, health care provider, or pharmacist first

  • Aducanumab has severe interactions with no other drugs.
  • Aducanumab has serious interactions with no other drugs.
  • Aducanumab has moderate interactions with no other drugs.
  • Aducanumab has minor interactions with no other drugs.

This information does not contain all possible interactions or adverse effects. Visit the RxList Drug Interaction Checker for any drug interactions. Therefore, before using this drug, tell your doctor or pharmacist of all the drugs you use. Keep a list of all your medications with you, and share the list with your doctor and pharmacist. Check with your physician if you have health questions or concerns.

What Are Warnings and Precautions For Aducanumab?


  • None

Effects of drug abuse

  • None

Short-Term Effects

  • See “What Are Side Effects Associated with Using Aducanumab?”

Long-Term Effects

  • See “What Are Side Effects Associated with Using Aducanumab?”


  • Angioedema and urticaria reported; promptly discontinue infusion upon first observation of any signs or symptoms consistent with a hypersensitivity reaction, and initiate appropriate therapy
  • Amyloid-related imaging abnormalities (ARIA)
    • May cause ARIA-E; observed on MRI as brain edema, sulcal effusions, and ARIA-H, which includes microhemorrhage and superficial siderosis
    • ARIA most commonly presents as temporary swelling in areas of the brain that usually resolves over time; other symptoms include headache, confusion, dizziness, vision changes, or nausea
    • The majority of ARIA was observed during the first 8 doses, particularly during titration; enhanced clinical vigilance recommended
    • Safety in patients with any pretreatment localized superficial siderosis, greater than 10 brain microhemorrhages, and/or with a brain hemorrhage  more than 1 cm within 1 year of treatment initiation has not been established
    • For ARIA-E or mild/moderate ARIA-H, continue treatment
    • If dosing is temporarily suspended, resume at same dose and titration schedule
    • There are no systematic data on continued dosing following the detection of radiographically moderate or severe ARIA
    • Refer to prescribing information for ARIA MRI classification criteria

Pregnancy and Lactation

  • There are no adequate data on use in pregnant females to evaluate for drug-associated risks of major birth defects, miscarriage, or other adverse maternal or fetal outcomes
  • No data are available on the presence of aducanumab in human milk, effects on breastfed infants, or effects on milk production

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